MedTech Summit 2020

Memo

Join hundreds of medical device, IVD and combination product professionals online on 12-16 October 2020 to get the latest regulatory insights and practical advice for implementing the EU MDR, IVDR and Global Market regulations, and more! Gather regulatory guidance and feedback direct from European Commission, Competent Authority and Notified Body representatives to gain clarification on the requirements and their expectations, and, benchmark your progress with leading industry case studies including strategic advice to help you ensure you're on track for compliance. Get all of your updates in one place with the opportunity to move between all of the conference tracks on the days you choose to attend:- EU Medical Device Regulation - 12-13 October 2020- EU Medical Device Law - 12 October 2020- Post Market Surveillance and Vigilance - 13-14 October 2020- Clinical Evaluations and Investigations - 13-14 October 2020- Medical Device Regulatory Affairs in Global Markets - 14-15 October 2020- Software and AI - 15 October 2020- EU IVD Regulation and Strategy - 15-16 October 2020- Biocompatibility for Medical Devices - 15-16 October 2020- Drug Device Combination Products - 16 October 2020- TRAINING COURSE: Medical Device Regulatory Project Management - 27-30 October 2020 Plus, benefit from AI-powered match-making, tech tour demos, one-to-one video meetings, interactive roundtable discussions, live Q and As, and the added bonus of 30-days of on-demand access to the speaker presentations - so you can re-watch the parts you found most valuable and catch up on presentations you missed. Build your 2, 3, 4 or 5 day pass and secure your place today. You will gain full access to all conference tracks and training courses on the days you choose to attend so be sure to take a look at the full 5 day agenda. For sponsorship and exhibition opportunities, please get in touch. URLs:Tickets: https://go.evvnt.com/601480-0?pid=5569Sponsor: https://go.evvnt.com/601480-3?pid=5569Twitter: https://go.evvnt.com/601480-4?pid=5569LinkedIn: https://go.evvnt.com/601480-5?pid=5569 Prices:2 Day Pass: GBP 950.0,3 Day Pass: GBP 1250.0,4 Day Pass: GBP 1500.0,5 Day Pass: GBP 1650.0 Speakers: Gavia Taan, Unit Manager - Devices Regulatory Policy Devices Division, MHRA, Augusto Geyer, Deputy General Manager, Medical Devices Office, ANVISA, Brazil, Sasikala Devi Thangavelu, Director, Policy, Code and Standard Division, Medical Device Authority, Ministry of Health, Malaysia, Elaine Darcy, European Medical Device Operations Manager, NSAI, Daniele Bollati, Product Conformity Assessment /Medical Devices Expert, IMQ, Andreas Stange, Vice President MHS global IVD, TUV SUD, Inge Vandenbussche, Director Regulatory Affairs EMEA, Medtronic, Erik Vollebregt, Partner, Axon Lawyers, The Netherlands, Maham Ansari, Director of Regulatory Affairs, Synaptive Medical, Canada, Bassil Akra, CEO, QUNIQUE GmbH, Germany, Jeremy Tinkler, Chairman of ISO/TC 194 (biological and clinical evaluation of medical devices) Director of Regulatory Consultancy and Quality Assurance at MedPass Intl, Yvonne Ndefo, Chief Clinical Evaluator, NSAI, Philippe Auclair, Senior Director, Regulatory Strategy and Advocacy, Abbott Quality and Regulatory, Abbott, Jessica Ward, Sr. Clinical Affairs Manager, Stryker, Mairead Finucane, Project Lead and Inspector for joint assessments of notified bodies (medical devices), DG Sante, European Commission, Juliana Witte, Clinical Evaluation Manager, Institut Straumann AG, Stephen Lee, MHRA, Alexandra Stamati, Director, Quality Assurance-PRRC, Medicon Hellas SA, Michaela Herron, Partner, Mason, Hayes and Curran, Ireland, Alex Denoon, Partner, Bristows LLP, UK, Giorgio Rizzello, Legal Director EMEA, Johnson and Johnson, Belgium, Nele Ooms, QA Manager, UgenTec, Pat Baird, Regulatory Head of Global Software Standards, Philips, Johan Ordish, Senior Policy Advisor, PHG Foundation, Georg Bauer, Department Manager Foreign Affairs, TUV SUD, Germany, Mercedes Bayani, Global Vice-President, Clinical and Regulatory Affairs, Bioness, USA, Alexey Stepanov, Quality Assurance and Regulatory Affairs Manager, Medical Devices in Russia, Russia, Sophie Clewlow, Higher Medical Device Specialist, MHRA, Khaudeja Bano, Executive Medical Director, Combination Product Safety Head, Amgen, Stephan Affolter, Regulatory + Quality Intelligence Manager, Ypsomed, Switzerland, Fran DeGrazio, Chief Scientific Officer, West Pharmaceutical Services, USA, And many more! Date and Time: On Monday October 12, 2020 at 10:30 am (ends Friday October 16, 2020 at 4:15 pm)